| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:103092044-103092261 | Common:1; Rare:69 | ||||
| chr11:103109336-103109577 | Common:1; Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:106077335-106077730 | Common:2; Rare:124 | ||||
| chr11:107457793-107457932 | Common:1; Rare:42 | ||||
| chr11:107565692-107565803 | Rare:33 | ||||
| chr11:108009113-108009163 | Rare:10 | ||||
| chr11:108009273-108009349 | Rare:38 | ||||
| chr11:108121404-108121628 | Common:5; Rare:77; Clinvar:1; Clinvar (benign):5 | ||||
| chr11:108222581-108223122 | Common:1; Rare:173; Clinvar:7; Clinvar (benign):1 | ||||
| chr11:108593749-108593880 | Common:2; Rare:40 | ||||
| chr11:108929330-108929621 | Common:1; Rare:52 | ||||
| chr11:110296507-110296753 | Rare:122; Clinvar:7 | ||||
| chr11:110430054-110430217 | Common:3; Rare:40 | ||||
| chr11:111541167-111541358 | Common:1; Rare:47 | ||||
| chr11:111541474-111541560 | Common:2; Rare:19 |